Effect of Hydroxychloroquine on QTc in Patients Diagnosed with COVID-19: A Systematic Review and Meta-Analysis.

COVID-19 QTc QTc prolongation SARS-CoV-2 chloroquine coronavirus hydroxychloroquine torsades de pointes

Journal

Journal of cardiovascular development and disease
ISSN: 2308-3425
Titre abrégé: J Cardiovasc Dev Dis
Pays: Switzerland
ID NLM: 101651414

Informations de publication

Date de publication:
13 May 2021
Historique:
received: 20 03 2021
revised: 25 04 2021
accepted: 08 05 2021
entrez: 2 6 2021
pubmed: 3 6 2021
medline: 3 6 2021
Statut: epublish

Résumé

Hydroxychloroquine or chloroquine with or without the concomitant use of azithromycin have been widely used to treat patients with SARS-CoV-2 infection, based on early in vitro studies, despite their potential to prolong the QTc interval of patients. This is a systematic review and metanalysis designed to assess the effect of hydroxychloroquine with or without the addition of azithromycin on the QTc of hospitalized patients with COVID-19. PubMed, Scopus, Cochrane and MedRxiv databases were reviewed. A random effect model meta-analysis was used, and I-square was used to assess the heterogeneity. The prespecified endpoints were ΔQTc, QTc prolongation > 500 ms and ΔQTc > 60 ms. A total of 18 studies and 7179 patients met the inclusion criteria and were included in this systematic review and meta-analysis. The use of hydroxychloroquine with or without the addition of azithromycin was associated with increased QTc when used as part of the management of patients with SARS-CoV-2 infection. The combination therapy with hydroxychloroquine plus azithromycin was also associated with statistically significant increases in QTc. Moreover, the use of hydroxychloroquine alone, azithromycin alone, or the combination of the two was associated with increased numbers of patients that developed QTc prolongation > 500 ms. This systematic review and metanalysis revealed that the use of hydroxychloroquine alone or in conjunction with azithromycin was linked to an increase in the QTc interval of hospitalized patients with SARS-CoV-2 infection that received these agents.

Sections du résumé

BACKGROUND BACKGROUND
Hydroxychloroquine or chloroquine with or without the concomitant use of azithromycin have been widely used to treat patients with SARS-CoV-2 infection, based on early in vitro studies, despite their potential to prolong the QTc interval of patients.
OBJECTIVE OBJECTIVE
This is a systematic review and metanalysis designed to assess the effect of hydroxychloroquine with or without the addition of azithromycin on the QTc of hospitalized patients with COVID-19.
MATERIALS AND METHODS METHODS
PubMed, Scopus, Cochrane and MedRxiv databases were reviewed. A random effect model meta-analysis was used, and I-square was used to assess the heterogeneity. The prespecified endpoints were ΔQTc, QTc prolongation > 500 ms and ΔQTc > 60 ms.
RESULTS RESULTS
A total of 18 studies and 7179 patients met the inclusion criteria and were included in this systematic review and meta-analysis. The use of hydroxychloroquine with or without the addition of azithromycin was associated with increased QTc when used as part of the management of patients with SARS-CoV-2 infection. The combination therapy with hydroxychloroquine plus azithromycin was also associated with statistically significant increases in QTc. Moreover, the use of hydroxychloroquine alone, azithromycin alone, or the combination of the two was associated with increased numbers of patients that developed QTc prolongation > 500 ms.
CONCLUSION CONCLUSIONS
This systematic review and metanalysis revealed that the use of hydroxychloroquine alone or in conjunction with azithromycin was linked to an increase in the QTc interval of hospitalized patients with SARS-CoV-2 infection that received these agents.

Identifiants

pubmed: 34068104
pii: jcdd8050055
doi: 10.3390/jcdd8050055
pmc: PMC8152730
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

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Auteurs

Angelos Arfaras-Melainis (A)

Jacobi Medical Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

Andreas Tzoumas (A)

School of Medicine, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.

Damianos G Kokkinidis (DG)

Section of Cardiovascular Medicine, Yale New Haven Hospital, Yale University School of Medicine, New Haven, CT 06510, USA.

Maria Salgado Guerrero (M)

Jacobi Medical Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

Dimitrios Varrias (D)

Jacobi Medical Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

Xiaobo Xu (X)

Jacobi Medical Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

Luis Cerna (L)

Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, NY 10467, USA.

Ricardo Avendano (R)

Section of Cardiovascular Medicine, Yale New Haven Hospital, Yale University School of Medicine, New Haven, CT 06510, USA.

Cameron Kemal (C)

Leon H. Charney Division of Cardiology, New York University, New York, NY 10016, USA.

Leonidas Palaiodimos (L)

Jacobi Medical Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

Robert T Faillace (RT)

Jacobi Medical Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

Classifications MeSH